About the ALS Association Alabama Chapter
The Alabama Chapter was founded in 2004 to serve the needs of all those affected by ALS disease. We provide patient programs, advocate on behalf of patients with our government leaders, create awareness of the disease, and fund research. In addition, the Chapter provides financial support to our statewide multidisciplinary ALS clinics and research facilities, enabling them to increase patient care.
The ALS Association is the ONLY national not-for-profit health organization dedicated solely to the fight against ALS. The ALS Association covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease.
Alongside the ALS Association National Office, the Alabama Chapter operates under a shared mission: to lead the fight to cure and treat ALS through global, cutting-edge research, and to empower people with Lou Gehrig's Disease and their families to live fuller lives by providing them with compassionate care and support.
Visit the ALS Association Alabama Chapter Website